UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (34) 34
humans (30) 30
life sciences & biomedicine (23) 23
genome-wide association study (21) 21
genetics & heredity (18) 18
genetic aspects (17) 17
genomes (15) 15
female (14) 14
polymorphism, single nucleotide (14) 14
male (13) 13
risk factors (13) 13
research (12) 12
case-control studies (11) 11
genetics (10) 10
multidisciplinary sciences (10) 10
science & technology - other topics (10) 10
genomics (9) 9
adult (8) 8
genetic predisposition to disease (8) 8
genotype (8) 8
medical research (8) 8
middle aged (8) 8
studies (8) 8
medicin och hälsovetenskap (7) 7
mutation (7) 7
physiological aspects (7) 7
aged (6) 6
gene expression (6) 6
genetic variation (6) 6
single nucleotide polymorphisms (6) 6
biochemistry & molecular biology (5) 5
eye diseases (5) 5
gene frequency (5) 5
genes (5) 5
genetic predisposition to disease - genetics (5) 5
health aspects (5) 5
klinisk medicin (5) 5
medical and health sciences (5) 5
polymorphism, single nucleotide - genetics (5) 5
psychiatry (5) 5
schizophrenia (5) 5
schizophrenia - genetics (5) 5
autoimmune diseases (4) 4
biomedical research (4) 4
cancer (4) 4
child (4) 4
disease (4) 4
disease susceptibility (4) 4
european continental ancestry group - genetics (4) 4
genome, human (4) 4
meta-analysis (4) 4
neurosciences (4) 4
quality control (4) 4
adolescent (3) 3
aged, 80 and over (3) 3
alleles (3) 3
analysis (3) 3
association analysis (3) 3
chromosomes (3) 3
clinical medicine (3) 3
cohort studies (3) 3
deoxyribonucleic acid--dna (3) 3
development and progression (3) 3
epidemiology (3) 3
european continental ancestry group (3) 3
genetic loci (3) 3
genetic structures (3) 3
glaucoma, open-angle - genetics (3) 3
histocompatibility antigens (3) 3
hla histocompatibility antigens (3) 3
hospitals (3) 3
major histocompatibility complex (3) 3
medicinsk genetik (3) 3
medicinska och farmaceutiska grundvetenskaper (3) 3
polymorphism, genetic - genetics (3) 3
quantitative trait loci (3) 3
quantitative trait, heritable (3) 3
sense organs (3) 3
tumors (3) 3
610 medicine & health (2) 2
animals (2) 2
ankylosing spondylitis (2) 2
asian continental ancestry group (2) 2
association studies (2) 2
australia (2) 2
bacteremia - genetics (2) 2
bacteremia - microbiology (2) 2
bacteremia - pathology (2) 2
biology (2) 2
bipolar disorder (2) 2
breast cancer (2) 2
breast neoplasms - genetics (2) 2
cancer and oncology (2) 2
cancer och onkologi (2) 2
card signaling adaptor proteins - genetics (2) 2
child, preschool (2) 2
cognition (2) 2
computational biology (2) 2
consortia (2) 2
core binding factor alpha 3 subunit - genetics (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Nik-Zainal, Serena and Davies, Helen and Staaf, Johan and Ramakrishna, Manasa and Glodzik, Dominik and Zou, Xueqing and Martincorena, Inigo and Alexandrov, Ludmil B and Martin, Sancha and Wedge, David C and Van Loo, Peter and Ju, Young Seok and Smid, Marcel and Brinkman, Arie B and Morganella, Sandro and Aure, Miriam R and Lingjærde, Ole Christian and Langerød, Anita and Ringnér, Markus and Ahn, Sung-Min and Boyault, Sandrine and Brock, Jane E and Broeks, Annegien and Butler, Adam and Desmedt, Christine and Dirix, Luc and Dronov, Serge and Fatima, Aquila and Foekens, John A and Gerstung, Moritz and Hooijer, Gerrit K. J and Jang, Se Jin and Jones, David R and Kim, Hyung-Yong and King, Tari A and Krishnamurthy, Savitri and Lee, Hee Jin and Lee, Jeong-Yeon and Li, Yilong and McLaren, Stuart and Menzies, Andrew and Mustonen, Ville and O’Meara, Sarah and Pauporté, Iris and Pivot, Xavier and Purdie, Colin A and Raine, Keiran and Ramakrishnan, Kamna and Rodríguez-González, F. Germán and Romieu, Gilles and Sieuwerts, Anieta M and Simpson, Peter T and Shepherd, Rebecca and Stebbings, Lucy and Stefansson, Olafur A and Teague, Jon and Tommasi, Stefania and Treilleux, Isabelle and Van den Eynden, Gert G and Vermeulen, Peter and Vincent-Salomon, Anne and Yates, Lucy and Caldas, Carlos and Veer, Laura van’t and Tutt, Andrew and Knappskog, Stian and Tan, Benita Kiat Tee and Jonkers, Jos and Borg, Åke and Ueno, Naoto T and Sotiriou, Christos and Viari, Alain and Futreal, P. Andrew and Campbell, Peter J and Span, Paul N and Van Laere, Steven and Lakhani, Sunil R and Eyfjord, Jorunn E and Thompson, Alastair M and Birney, Ewan and Stunnenberg, Hendrik G and van de Vijver, Marc J and Martens, John W. M and Børresen-Dale, Anne-Lise and Richardson, Andrea L and Kong, Gu and Thomas, Gilles and Stratton, Michael R and Los Alamos National Lab. (LANL), Los Alamos, NM (United States)
Nature (London), ISSN 1476-4687, 05/2016, Volume 534, Issue 7605, pp. 47 - 54
Journal Article
by Su, Zhan and Gay, Laura J and Strange, Amy and Palles, Claire and Band, Gavin and Whiteman, David C and Lescai, Francesco and Langford, Cordelia and Nanji, Manoj and Edkins, Sarah and van der Winkel, Anouk and Levine, David and Sasieni, Peter and Bellenguez, Céline and Howarth, Kimberley and Freeman, Colin and Trudgill, Nigel and Tucker, Art T and Pirinen, Matti and Peppelenbosch, Maikel P and van der Laan, Luc J W and Kuipers, Ernst J and Drenth, Joost P H and Peters, Wilbert H and Reynolds, John V and Kelleher, Dermot P and McManus, Ross and Grabsch, Heike and Prenen, Hans and Bisschops, Raf and Krishnadath, Kausila and Siersema, Peter D and van Baal, Jantine W P M and Middleton, Mark and Petty, Russell and Gillies, Richard and Burch, Nicola and Bhandari, Pradeep and Paterson, Stuart and Edwards, Cathryn and Penman, Ian and Vaidya, Kishor and Ang, Yeng and Murray, Iain and Patel, Praful and Ye, Weimin and Mullins, Paul and Wu, Anna H and Bird, Nigel C and Dallal, Helen and Shaheen, Nicholas J and Murray, Liam J and Koss, Konrad and Bernstein, Leslie and Romero, Yvonne and Hardie, Laura J and Zhang, Rui and Winter, Helen and Corley, Douglas A and Panter, Simon and Risch, Harvey A and Reid, Brian J and Sargeant, Ian and Gammon, Marilie D and Smart, Howard and Dhar, Anjan and McMurtry, Hugh and Ali, Haythem and Liu, Geoffrey and Casson, Alan G and Chow, Wong-Ho and Rutter, Matt and Tawil, Ashref and Morris, Danielle and Nwokolo, Chuka and Isaacs, Peter and Rodgers, Colin and Ragunath, Krish and MacDonald, Chris and Haigh, Chris and Monk, David and Davies, Gareth and Wajed, Saj and Johnston, David and Gibbons, Michael and Cullen, Sue and Church, Nicholas and Langley, Ruth and Griffin, Michael and Alderson, Derek and Deloukas, Panos and Hunt, Sarah E and Gray, Emma and Dronov, Serge and Potter, Simon C and Tashakkori-Ghanbaria, Avazeh and Anderson, Mark and Brooks, Claire and Blackwell, Jenefer M and Bramon, Elvira and ... and Wellcome Trust Case Control Consor and Esophageal Adenocarcinoma Genetics and Wellcome Trust Case Control Consortium 2 and Esophageal Adenocarcinoma Genetics Consortium and The Wellcome Trust Case Control Consortium 2 and The Esophageal Adenocarcinoma Genetics Consortium
Nature genetics, ISSN 1061-4036, 09/2012, Volume 44, Issue 10, pp. 1131 - 1136
Journal Article
Nature communications, ISSN 2041-1723, 05/2018, Volume 9, Issue 1, pp. 1864 - 11
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Lumican - metabolism | Glaucoma, Open-Angle - genetics | Humans | Corneal Diseases - metabolism | Corneal Dystrophies, Hereditary - ethnology | Corneal Diseases - genetics | Ehlers-Danlos Syndrome - genetics | Corneal Dystrophies, Hereditary - pathology | Loeys-Dietz Syndrome - metabolism | Mendelian Randomization Analysis | Fibrillin-1 - metabolism | Cornea - pathology | Keratoconus - pathology | Corneal Diseases - pathology | Decorin - genetics | Gene Expression | Eye Diseases, Hereditary - pathology | Lumican - genetics | ADAMTS Proteins - metabolism | Proteoglycans - metabolism | Ehlers-Danlos Syndrome - ethnology | European Continental Ancestry Group | Myopia - pathology | Cornea - metabolism | Myopia - ethnology | Loeys-Dietz Syndrome - pathology | Corneal Diseases - ethnology | Marfan Syndrome - metabolism | Marfan Syndrome - pathology | Cornea - abnormalities | Quantitative Trait Loci | Proteoglycans - genetics | ADAMTS Proteins - genetics | Transforming Growth Factor beta2 - metabolism | Corneal Dystrophies, Hereditary - genetics | Glaucoma, Open-Angle - pathology | Keratoconus - metabolism | Loeys-Dietz Syndrome - ethnology | Glaucoma, Open-Angle - ethnology | Myopia - metabolism | Ehlers-Danlos Syndrome - pathology | Marfan Syndrome - ethnology | Keratoconus - genetics | Glaucoma, Open-Angle - metabolism | Fibrillin-1 - genetics | Eye Diseases, Hereditary - ethnology | Genome-Wide Association Study | Quantitative Trait, Heritable | Corneal Dystrophies, Hereditary - metabolism | Marfan Syndrome - genetics | Eye Diseases, Hereditary - genetics | Myopia - genetics | Asian Continental Ancestry Group | Keratoconus - ethnology | Ehlers-Danlos Syndrome - metabolism | Loeys-Dietz Syndrome - genetics | Polymorphism, Single Nucleotide | Transforming Growth Factor beta2 - genetics | Genome, Human | Decorin - metabolism | Eye Diseases, Hereditary - metabolism | Glaucoma | Cornea | Genes | Myopia | Association analysis | Genomes | Gene expression | Tissues | Connective tissues | Keratoconus | Collagen | Eye diseases | Extracellular matrix | Index Medicus
Journal Article
Nature methods, ISSN 1548-7105, 07/2013, Volume 10, Issue 8, pp. 723 - 729
Journal Article
Nature genetics, ISSN 1546-1718, 01/2013, Volume 45, Issue 2, pp. 208 - 213
Journal Article
Nature communications, ISSN 2041-1723, 07/2014, Volume 5, Issue 1, pp. 4204 - 4204
..., Richard Pearson3, Damjan Vukcevic3, Cordelia Langford8, Panos Deloukas8, Sarah Hunt8, Emma Gray8, Serge Dronov8, Simon C. Potter8, Avazeh Tashakkori-Ghanbaria8, Sarah... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetics, Population | Twins - genetics | Genome-Wide Association Study | Quantitative Trait, Heritable | Humans | Male | United Kingdom | Mathematics | Dyslexia - genetics | Learning | Twins - psychology | Reading | Dyslexia - psychology | Female | Polymorphism, Single Nucleotide | Child | Index Medicus
Journal Article
by Ripke, Stephan and O'Dushlaine, Colm and Chambert, Kimberly and Moran, Jennifer L and Kähler, Anna K and Akterin, Susanne and Bergen, Sarah E and Collins, Ann L and Crowley, James J and Fromer, Menachem and Kim, Yunjung and Lee, Sang Hong and Magnusson, Patrik K E and Sanchez, Nick and Stahl, Eli A and Williams, Stephanie and Wray, Naomi R and Xia, Kai and Bettella, Francesco and Borglum, Anders D and Bulik-Sullivan, Brendan K and Cormican, Paul and Craddock, Nick and de Leeuw, Christiaan and Durmishi, Naser and Gill, Michael and Golimbet, Vera and Hamshere, Marian L and Holmans, Peter and Hougaard, David M and Kendler, Kenneth S and Lin, Kuang and Morris, Derek W and Mors, Ole and Mortensen, Preben B and Neale, Benjamin M and O'Neill, Francis A and Owen, Michael J and Milovancevic, Milica Pejovic and Posthuma, Danielle and Powell, John and Richards, Alexander L and Riley, Brien P and Ruderfer, Douglas and Rujescu, Dan and Sigurdsson, Engilbert and Silagadze, Teimuraz and Smit, August B and Stefansson, Hreinn and Steinberg, Stacy and Suvisaari, Jaana and Tosato, Sarah and Verhage, Matthijs and Walters, James T and Bramon, Elvira and Corvin, Aiden P and O'Donovan, Michael C and Stefansson, Kari and Scolnick, Edward and Purcell, Shaun and McCarroll, Steven A and Sklar, Pamela and Hultman, Christina M and Sullivan, Patrick F and Wellcome Trust Case Control Consortium 2 and Multicenter Genetic Studies of Schizophrenia Consortium and Psychosis Endophenotypes International Consortium and Multictr Genetic Studies Schizophr and Wellcome Trust Case Control Consor and Psychosis Endophenotypes Int Conso
Nature genetics, ISSN 1546-1718, 08/2013, Volume 45, Issue 10, pp. 1150 - 1159
Journal Article